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4-Hexenal, 6-oxo-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

200624-53-9

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200624-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200624-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,6,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 200624-53:
(8*2)+(7*0)+(6*0)+(5*6)+(4*2)+(3*4)+(2*5)+(1*3)=79
79 % 10 = 9
So 200624-53-9 is a valid CAS Registry Number.

200624-53-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name O=CHCH2CH2CH=CH(C=O)Ph

1.2 Other means of identification

Product number -
Other names 6-oxo-6-phenylhex-4-enal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:200624-53-9 SDS

200624-53-9Relevant academic research and scientific papers

Catalysis of intramolecular Morita-Baylis-Hillman and Rauhut-Currier reactions by fluorous phosphines; facile recovery by liquid/solid organic/fluorous biphase protocols involving precipitation, teflon tape, and Gore-Rastex fiber

Seidel, Florian O.,Gladysz, John A.

, p. 2443 - 2449 (2008)

The fluorous phosphine P[(CH2)3Rf8] 3 [1, Rf8=(CF2)7CF3; 10 mol%] catalyzes intramolecular Morita-Baylis-Hillman reactions of O=CH-(CH 2)nCH=CH(C=O)R [n/R=2/Ph (2a), 2/S-i-Pr, 3/p-tol] in acetonitrile at 60-72°C. Upon cooling, 1 precipitates and is recycled. The products HOCH(CH2)nCH=C(C=O)R are isolated from the supernatant (78-96%). The educt i-PrS(C=O)CH=CH(CH2) 2CH=CH(C=O)S-i-Pr similarly undergoes a Rauhut-Currier reaction to give i-PrS(C=O)CH2CH(CH2)2CH=C(C=O)S-i-Pr (71-73%). In the case of 2a, reactions are also conducted in the presence of Teflon tape or Gore-Rastex fiber. The catalyst now precipitates onto the fluoropolymer support, mechanically facilitating recycling. For each reaction, three to five cycles are conducted. HPLC or GC monitoring of the rates show low activity losses, with Gore-Rastex fiber giving better results than Teflon tape, presumably due to a higher surface area.

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